A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5457937



Internal ID235972
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:166328535..166331020hg38UCSC Ensembl
chr6:166742023..166744508hg19UCSC Ensembl
Cytoband6q27
Allele length
AssemblyAllele length
hg382486
hg192486
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv16991001
Samples
Known GenesSFT2D1
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nsv5457937
Frequency
Sample Size3202
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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